MedPath

Benzo-Jel

BENZO-JEL™

Approved
Approval ID

614dce60-99f4-45e5-8b7b-e84240a34e8f

Product Type

HUMAN PRESCRIPTION DRUG LABEL

Effective Date

May 1, 2015

Manufacturers
FDA

Henry Schein Inc

DUNS: 012430880

Products 1

Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.

Benzocaine

Product Details

FDA regulatory identification and product classification information

FDA Identifiers
NDC Product Code0404-0436
Product Classification
G
Generic Name
Benzocaine
Product Specifications
Route of AdministrationDENTAL
Effective DateMay 1, 2015
FDA Product Classification

INGREDIENTS (1)

BenzocaineActive
Quantity: 230 mg in 1 mL
Code: U3RSY48JW5
Classification: ACTIB

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